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Radiographic Evaluation of a Star-shaped Incision Technique

Radiographic Evaluation of a Star-shaped Incision Technique for Thick-gingiva and Thin-gingiva Patients Treated With Implant-supported Fixed Prosthesis: a Randomized Trial

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05190614
Enrollment
24
Registered
2022-01-13
Start date
2019-06-01
Completion date
2021-06-01
Last updated
2022-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Clinical and Radiographic Effect, Implant, Thick-gingiva, Thin-gingiva

Brief summary

To evaluate a star-shaped incision technique to thick-gingiva and thingingiva patients treated with implant-supported fixed prosthesis. The star-shaped incision would be an effective and simple method to reconstruct gingival papillae and avoid the gingival recession in thick-gingiva patients treated with implant-supported fixed prosthesis, and it is worthy of clinical extend.

Detailed description

Objective: To evaluate a star-shaped incision technique to thick-gingiva and thin-gingiva patients treated with implant-supported fixed prosthesis. Methods and Materials: 24 patients received cross-shaped incision were assigned into thick-gingiva group (16 cases) and thin-gingiva group (8 cases). Follow-up examination was carried out 3 and 12 months after final restoration. Clinical and radiographic evaluation including gingival papilla height, modified plaque index, modified sulcus bleeding index, periodontal depth, and crestal marginal bone level were utilized.

Interventions

DIAGNOSTIC_TESTThe biotype of gingiva

The biotype of gingival was determined by periodontal probe.

Sponsors

Wen Luo
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
22 Years to 58 Years
Healthy volunteers
Yes

Inclusion criteria

1. Good general health, no chronic systemic diseases. 2. All subjects included in this study needed to have one missing premolar or molar teeth with adjacent natural teeth. 3. All subjects included in this study had been treated with one bone-level implant insertion in the premolar or molar region. The patients had insufficient gingival papilla height (referred to contralateral natural tooth which also had insufficient gingival papilla height) and at least 2 mm of keratinized tissue width around the implant.

Exclusion criteria

1. Active periodontal infections. 2. Heavy smoking (\> 10 cigarettes per day).

Design outcomes

Primary

MeasureTime frameDescription
Papilla heightBetween June 2019 and June 2021Presence/absence of papilla height was assessed visually according to the papilla index proposed by Jemt
Modified Plaque Index (mPI)Between June 2019 and June 2021plaque accumulation around the marginal peri-implant tissue was assessed by the criteria of mPI
Modified Sulcus Bleeding Index (mBI)Between June 2019 and June 2021the bleeding tendency of the marginal peri-implant tissue was evaluated using mBI
Probing Depth (PD, mm)Between June 2019 and June 2021PD was assessed at the mid-buccal, mid-oral, mesial and distal aspects of the buccal surfaces of each implant with a standard periodontal probe, and final value was determined by the average of four aspects.
Gingival margin level (GML)Between June 2019 and June 2021gingival margin level was assessed by calculating the vertical distance between the most apical point of gingival margin at the buccal aspect of the crown and line connecting the peak of the adjacent mesial and distal natural teeth (PMD)
The landmarks of first bone-implant contact (fBIC) and implant shoulder (IS)Between June 2019 and June 2021fBIC-IS was defined as the vertical distance the first bone-implant contact to implant shoulder, and the distance was assessed at the mesial and distal aspect of implant, respectively. When the marginal crestal bone was located coronal to the IS, a positive (+) value was given, where a negative (-) value when located apically to the IS, the value was deemed as zero when IS and fBIC coincided. The crestal bone level at the time of impression taking was regarded as baseline. The known implant length was used for the calibration of dimensional distortion in the radiograph (the length of implant was 10 mm).

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026